UREA - India CDSCO Medical Device Registration

UREA is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/MD/2018/000023_add5bb609656fa2768c6e834c7b4a643_53e0c177cc7145d12e35d38171c55345. This device is marketed under the brand name AUTOPAK™. The license holder is Siemens Healthcare Private Limited, and it is classified as Device Class Class B. The approving authority is Gujarat.

This page provides comprehensive regulatory information including complete registration details, license holder information, device classification, and related products. Pure Global AI offers free access to 71,807+ India medical device registrations, helping global MedTech companies identify partners, analyze markets, and discover business opportunities efficiently.

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CDSCO Registered

Class Class B

UREA

UID: MFG/MD/2018/000023_add5bb609656fa2768c6e834c7b4a643_53e0c177cc7145d12e35d38171c55345

Brand Name

AUTOPAK™

License Holder

Siemens Healthcare Private Limited

Device Class

Class B

Approving Authority

Gujarat

Product Information

For In vitro diagnostics use in quantitative determination of Urea in serum or plasma using clinical chemistry analyzer

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CALCIUM- Cyanide Free

Brand: AUTOPAK™

Siemens Healthcare Private Limited

UREA - India CDSCO Medical Device Registration

Brand Name

License Holder

Device Class

Approving Authority

Product Information

DJ Fang

CALCIUM- Cyanide Free

Protein, pH, Specific Gravity

Protein, pH, Specific Gravity

CHOLINESTERASE

HbA1c Calibrator

HbA1c

Albumin

Total Protein

LDH Liquid Stable

Direct Bilirubin Vanadate

CALCIUM- Cyanide Free

Protein, pH, Specific Gravity

Protein, pH, Specific Gravity

CHOLINESTERASE

HbA1c Calibrator

HbA1c

Albumin

Total Protein

LDH Liquid Stable

Direct Bilirubin Vanadate